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27. Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity. Risinger M; Christakopoulos GE; Schultz CL; McGann PT; Zhang W; Kalfa TA Pediatr Blood Cancer; 2019 Feb; 66(2):e27531. PubMed ID: 30393954 [TBL] [Abstract][Full Text] [Related]
28. [Elliptocytosis--hereditary elliptocytotic anemia in a 12-year-old girl]. Pavkovceková O; Cesnak D; Prekop R Cesk Pediatr; 1969 Oct; 24(10):931-5. PubMed ID: 5406572 [No Abstract] [Full Text] [Related]
29. Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis. Al-Riyami AZ; Iolascon A; Al-Zadjali S; Andolfo I; Al-Mammari S; Manna F; Al Rawas A; King MJ; Russo R Am J Hematol; 2017 Oct; 92(10):E607-E609. PubMed ID: 28699249 [No Abstract] [Full Text] [Related]
30. Homozygous hereditary elliptocytosis as the cause of haemolytic anemia in infancy. Nielsen JA; Praktitioner S Scand J Haematol; 1968; 5(6):486-96. PubMed ID: 5731934 [No Abstract] [Full Text] [Related]
31. Hereditary elliptocytosis with haemolytic crisis following infection. A case report. Obe JA; Akinyanju OO Niger Med J; 1978 Sep; 8(5):461-4. PubMed ID: 735409 [No Abstract] [Full Text] [Related]
32. Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia. Gallagher PG; Petruzzi MJ; Weed SA; Zhang Z; Marchesi SL; Mohandas N; Morrow JS; Forget BG J Clin Invest; 1997 Jan; 99(2):267-77. PubMed ID: 9005995 [TBL] [Abstract][Full Text] [Related]
33. Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site. Gallagher PG; Zhang Z; Morrow JS; Forget BG Lab Invest; 2004 Feb; 84(2):229-34. PubMed ID: 14661034 [TBL] [Abstract][Full Text] [Related]
34. A family affair-Severe fetal and neonatal hemolytic anemia due to novel alpha-spectrin mutations in two siblings. Donepudi R; Westerfield L; Stonecipher A; A Nassr A; Cortes MS; Espinoza J; Belfort M; Shamshirsaz A Am J Med Genet A; 2020 Mar; 182(3):561-564. PubMed ID: 31854503 [TBL] [Abstract][Full Text] [Related]
35. Novel compound heterozygous SPTA1 mutations in a patient with hereditary elliptocytosis. Ma S; Qin J; Wei A; Li X; Qin Y; Liao L; Lin F Mol Med Rep; 2018 Apr; 17(4):5903-5911. PubMed ID: 29484404 [TBL] [Abstract][Full Text] [Related]
36. Novel mutations in patients with hereditary red blood cell membrane disorders using next-generation sequencing. He Y; Jia S; Dewan RK; Liao N Gene; 2017 Sep; 627():556-562. PubMed ID: 28694211 [TBL] [Abstract][Full Text] [Related]